| 9|c|Proton kinematics | ||||||||
|---|---|---|---|---|---|---|---|---|
| Ee | Q2 | Proton | Proton | |||||
| (GeV) | (GeV)2 | (deg) | K.E.(GeV) | Momentum | (cm2/msr) | %/deg | %/(%Ee) | |
|
1.162 |
0.50 | .762 | 50.407 | 0.266 | 0.756 | 4.540e-32 | 13.26 | 4.22 |
|
1.162 |
1.45 | .081 | 12.540 | 0.773 | 1.431 | 1.640e-33 | 3.65 | 4.00 |
|
2.262 |
0.50 | .939 | 60.075 | 0.266 | 0.756 | 6.373e-32 | 18.56 | 4.67 |
|
2.262 |
1.45 | .746 | 40.175 | 0.773 | 1.431 | 2.334e-33 | 14.68 | 5.36 |
|
2.262 |
3.20 | .131 | 12.525 | 1.705 | 2.471 | 1.227e-34 | 5.51 | 4.43 |
|
3.362 |
0.50 | .973 | 63.191 | 0.266 | 0.756 | 7.238e-32 | 20.93 | 4.83 |
|
3.362 |
3.20 | .610 | 28.048 | 1.705 | 2.471 | 1.429e-34 | 14.08 | 5.48 |
|
3.362 |
4.90 | .181 | 12.664 | 2.611 | 3.423 | 2.617e-35 | 7.34 | 4.58 |
|
5.562 |
0.50 | .990 | 65.664 | 0.266 | 0.756 | 8.050e-32 | 23.16 | 4.97 |
|
5.562 |
1.45 | .963 | 50.864 | 0.773 | 1.431 | 3.227e-33 | 20.71 | 6.13 |
|
5.562 |
3.20 | .871 | 36.255 | 1.705 | 2.471 | 1.751e-34 | 19.17 | 6.30 |
|
5.562 |
4.90 | .722 | 26.942 | 2.611 | 3.423 | 3.143e-35 | 17.48 | 5.91 |
| 9|c|Electron kinematics | ||||||||
| Ee | Q2 | Electron | ||||||
| (GeV) | (GeV)2 | (deg) | K.E.(GeV) | (cm2/msr) | %/deg | %/(%Ee) | ||
|
1.162 |
0.50 | .762 | 40.557 | 0.896 | 0.973 | 4.064e-32 | 14.70 | 8.69 |
|
1.162 |
1.45 | .081 | 127.062 | 0.389 | 0.991 | 1.185e-34 | 2.40 | 10.07 |
|
2.262 |
0.50 | .939 | 19.158 | 1.996 | 0.969 | 2.217e-31 | 33.19 | 8.98 |
|
2.262 |
1.45 | .746 | 38.299 | 1.489 | 0.934 | 1.933e-33 | 18.20 | 11.77 |
|
2.262 |
3.20 | .131 | 105.695 | 0.557 | 0.988 | 6.077e-36 | 3.62 | 11.49 |
|
3.362 |
0.50 | .973 | 12.584 | 3.096 | 0.969 | 5.479e-31 | 51.20 | 9.05 |
|
3.362 |
3.20 | .610 | 44.541 | 1.657 | 0.949 | 5.667e-35 | 15.20 | 13.06 |
|
3.362 |
4.90 | .181 | 88.315 | 0.751 | 0.987* | 1.228e-36 | 4.92 | 12.08 |
|
5.562 |
0.50 | .990 | 7.470 | 5.296 | 0.969 | 1.629e-30 | 87.01 | 9.09 |
|
5.562 |
1.45 | .963 | 13.398 | 4.789 | 0.919 | 2.282e-32 | 59.89 | 12.59 |
|
5.562 |
3.20 | .871 | 22.269 | 3.857 | 0.930 | 3.438e-34 | 37.05 | 14.24 |
|
5.562 |
4.90 | .722 | 31.710 | 2.951 | 0.950* | 1.751e-35 | 23.69 | 14.20 |
| 4r*assumes GE/GM = 0.45 at Q2=4.90 |
For this measurement, proton detection has several advantages over electron
detection. Protons at moderately large angles correspond to forward angle
electrons. Detecting the proton allows us to go to lower values of electron
scattering angle, down to ![]()
for this proposal, than would
normally be possible. It also reduces the effect of uncertainty in the measured
scattering angle. The cross section for forward angle electrons varies
rapidly with scattering angle, while the cross section dependence for the
corresponding protons is smaller by a factor of 2-3 for the kinematics where
this is a dominant source of uncertainty (as seen in Table 1). The reverse is
true for the backwards angle electrons: the angular variation of the cross
section is greater for the protons. However, it is a much smaller effect than
for the forwards angle electrons, and therefore the increased kinematical
dependence does not increase the overall uncertainty in the extracted form
factors. The limitation for backwards angle electrons is the reduced cross
section within the angular acceptance of the spectrometer. Again, measuring
the proton leads to a significant improvement, as the forward angle protons
are in a narrow angular range compared to the corresponding backwards angle electrons.
Finally, detection of the proton reduces the cross section variation with beam
energy for all kinematics.
In addition to the kinematic advantages of detecting the proton, the systematic
uncertainties in the Rosenbluth separation are smaller when the proton is
measured. This is due to the fact that the proton momentum is the same for
all
values at a given Q2. Thus the magnets are not set to
different currents when
is changed (which could lead to small
modifications to the optics), and momentum
dependence corrections such as detector efficiency and multiple scattering
will be nearly identical for the forwards and backwards angle measurements.
While there will be small angle-dependent differences in multiple scattering
due to the target geometry, the proton momentum will be identical, making
the differences smaller than the would be if the electron were detected.
The effect of any rate dependent efficiencies on the separation will also be
reduced because the difference in cross sections between forward and backwards
angles is much smaller than in the case where the electron is detected.
Finally, because the scattered electron is not detected, the radiative
corrections are significantly smaller (on average by a factor of two).
There will be corrections to the absolute cross section that are larger for
measured protons, but for the most part these cancel in the ratios. Proton
absorption in the target and spectrometer leads to a correction of a few
percent. However, the absorption in the spectrometer will completely cancel
when comparing the different
values, as the proton momentum is
identical at all kinematics. There will be a difference absorption in the
target because the amount of target material seen by the outgoing proton
depends on the scattering angle. For the standard 'beer can' target (4cm
length, 6.35cm diameter), the path length through the target varies between
2cm and 3.76cm, which gives a maximum difference of 0.26% in the proton
absorption. This will be even smaller if improved target cells (with a
smaller diameter) or 'tuna can' cells are used. The target geometry is taken
into account in the simulation, and this small difference in absorption can be
taken into account in the analysis, with a negligible uncertainty in the final
result.
Protons are not always stopped by the HRS collimator, so one
can not rely on the collimator to define the solid angle for the measurement.
We will define the solid angle using cuts on the reconstructed scattering
angles, in a region where the HRS has nearly complete acceptance.
While any error in the angular reconstruction will lead to an
uncertainty in the absolute solid angle, identical cuts will be used at
forwards and backwards angle, and so much of the uncertainty in the solid
angle will cancel. As the spectrometer angle changes, the length of the
target as seen by the HRS also changes. Thus, any target position
dependence of the reconstruction can lead to a change in solid angle.
We will measure this position dependence with sieve slit and elastic runs
on a 15cm target and the variable z-position optics targets, and use this to
correct for target length variation with scattering angle. The high Q2
data is taken at smaller scattering angles, where the target length dependence
should not be a large problem. The Q2=0.5 GeV2 normalization points are
taken at larger angles but the angle difference between the high and low
points are small. The change in target length as seen by the HRS
is <20% for the Q2=1.45 point, and
5% for the other
kinematics). The Q2=1.45 GeV2 point does have a large change in
scattering angle (from 12.5
to 51
), and we will have to rely on
measurement of the solid angle dependence to determine the size of the
correction. While we will have to measure the position dependence before we
know the size of the correction (and uncertainty), we will assume an
additional uncertainty of 0.5% to the acceptance for the Q2=1.45 GeV2
point to take into account the larger potential solid angle variation.
Once we have measured the solid angle dependence on target position, we
may well be able to correct to better than 0.5%, but we would like to
note that even if the uncertainty turns out to be twice as large, the
uncertainty on the extracted value of GE/GM at this Q2 is still
0.03, smaller than the uncertainty in the polarization transfer
measurement, and 6 standard deviations from unity if the Hall A result
is correct.